grant

Using a 24-Hour Movement Framework to Improve Pregnancy Outcomes

Organization KAISER FOUNDATION RESEARCH INSTITUTELocation Oakland, UNITED STATESPosted 1 Aug 2022Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY20240-11 years oldACRP30 proteinAccelerometerAdult-Onset Diabetes MellitusAffectAwardBehaviorBiological MarkersBirth WeightChildChild YouthChildren (0-21)Chronologic Fetal MaturityD-GlucoseDataData AnalysesData AnalysisData CollectionDevelopmentDevicesDextroseEPH GestosisEpidemiologyExposure toFetal AgeFundingGeneral PopulationGeneral PublicGeneralized GrowthGestationGestational AgeGestational DiabetesGestational Diabetes MellitusGlucoseGoalsGrowthGuidelinesHealthHourHumulin RIndividualInfantInsulinInsulin ResistanceInterventionIntervention StrategiesInvestigationInvestigatorsKetosis-Resistant Diabetes MellitusLate pregnancyLeptinLipidsMaturity-Onset Diabetes MellitusMeasurementMeasuresMentorsMentorshipMetabolicMovementNIDDMNatureNon-Insulin Dependent DiabetesNon-Insulin-Dependent Diabetes MellitusNoninsulin Dependent DiabetesNoninsulin Dependent Diabetes MellitusNovolin ROb Gene ProductOb ProteinObese Gene ProductObese ProteinObesityOutcomeOver weightOvernutritionOverweightPathway interactionsPatternPerinatalPeripartumPhasePhysical activityPhysiologyPolysomnographyPre-EclampsiaPreeclampsiaPregnancyPregnancy ComplicationsPregnancy OutcomePregnancy ToxemiasPregnancy-Induced DiabetesPregnant WomenPremature BirthPrematurely deliveringPreterm BirthProteinuria-Edema-Hypertension GestosisPublic HealthRecommendationRegular InsulinResearchResearch ActivityResearch PersonnelResearchersRiskRisk FactorsRoleSedentary behaviorSedentary life-styleSleepSleep MonitoringSlow-Onset Diabetes MellitusSomnographyStable Diabetes MellitusT2 DMT2DT2DMTimeTissue GrowthTrainingTraining ActivityType 2 Diabetes MellitusType 2 diabetesType II Diabetes MellitusType II diabetesUnited StatesWeightWomanWorkaccelerometryactivity monitoractivity trackeradipocyte complement-related protein 30-kDaadipocyte, C1q and collagen domain containing proteinadiponectinadiposityadult onset diabetesadverse pregnancy outcomeagedapM-1 proteinapM1 (adipose-specific) proteinbio-markersbiologic markerbiomarkerbody movementcardiometabolic riskchild adipositychild obesitychildhood adipositychildhood obesityclinical developmentcohortcomplications during pregnancycorpulencecritical perioddata interpretationdevelopmentaldiabetes riskearly biomarkersearly detection biomarkersearly detection markersearly pregnancyepidemiologicepidemiologicalexpectant motherexpecting motherexposed in uterofetal exposureglucose tolerancehigh risk grouphigh risk individualhigh risk peoplehigh risk populationimprovedin uteroin utero exposureinnovateinnovationinnovativeinsulin resistantinsulin toleranceinterventional strategyintra-uterine environmental exposureintrauterine environmental exposureketosis resistant diabeteskidsmaternal adipositymaternal obesitymaturity onset diabetesmetabolic profileneonatal adipositynewborn adipositynewborn obesityobese childrenobesity during childhoodobesity in childrenobesity preventionobesity riskontogenypathwaypediatric obesityperinatal outcomespolysomnographicpre-eclampticpregnancy diabetespregnancy toxemia/hypertensionpregnancy-related complicationspregnant motherspremature childbirthpremature deliveryprenatal exposureprenatally exposedpreterm deliverypreventprevent obesitypreventingrecruitreproductiveresearch studyrisk for obesityrisk mitigationrisk of obesitysedentary lifestyleskillssleep behaviorsleep habitsleep measurementsleep physiologysleep polysomnographysocial roletraining moduletype 2 DMtype II DMtype two diabetesvigorous intensityweightsyoungster
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Full Description

PROJECT SUMMARY/ABSTRACT
Maternal obesity, gestational diabetes, and childhood obesity are part of a vicious cycle. Almost half of all

reproductive-aged women in the United States are overweight or obese. Overweight and obese women are up

to 6 times more likely to develop GDM than normal weight women. Children exposed to GDM in utero have an

8-fold greater type 2 diabetes risk and a 2-fold greater obesity risk, perpetuating the cycle. Increasing physical

activity and sleep during pregnancy may help mitigate these risks. These behaviors are interrelated: improving

one (e.g. getting more physical activity) could occur at the expense of another (e.g. getting enough sleep). The

ideal daily pattern of physical activity and sleep to prevent pregnancy complications and subsequent childhood

obesity risk factors is unknown. Despite the interrelated nature of these behaviors, prior research on physical

activity, sedentary behavior, and sleep during pregnancy in overweight and obese pregnanct women has

focused on individual associations of these behaviors with perinatal outcomes. How the interdependent

relationships between physical activity, sedentary behavior, and sleep within a 24-hour movement framework

affect perinatal outcomes remains unclear. The goal of this K99/R00 Pathway to Independence Award is to

facilitate my transition to becoming an independent researcher with expertise in the 24-hour movement

framework during pregnancy to ultimately develop interventions and guidelines for 24-hour movement during

this critical period. During the Mentored (K99) Phase of this award, I will pursue training in the analysis of

accelerometer-measured physical activity data, the physiology and measurement of sleep, and practical skills

in research study conduct, including recruitment and retention, under the mentorship of Dr. Monique

Hedderson (Primary Mentor), Dr. Kelley Pettee Gabriel (Co-Mentor and expert in accelerometer-measured

physical activity within a 24-hour movement framework), and Dr. Rachel Manber (Co-Mentor and expert in

sleep during pregnancy). My research during the Mentored Phase will 1) assess whether 24-hour movement

profiles during early pregnancy are associated with late pregnancy maternal metabolic biomarkers, and 2)

assess whether 24-hour movement profiles during early and late pregnancy are associated with delivering

infants with childhood obesity risk factors using data from an existing study among overweight and obese

pregnant women. In the Independent (R00) Phase of this award, I will examine longitudinal relationships of 24-

hour movement profiles during pregnancy with glucose tolerance, birthweight, and neonatal adiposity by

creating a cohort of overweight and obese pregnant women with daily, device-based measurement of physical

activity, sedentary behavior, and sleep across pregnancy. These training and research activities will prepare

me to successfully compete for R01 funding to support further investigation of 24-hour movement profiles and

pregnancy outcomes in high-risk populations of pregnant women.

Grant Number: 5R00HD100585-05
NIH Institute/Center: NIH

Principal Investigator: Sylvia Badon

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